NDC 65862-144 – Carvedilol

Carvedilol 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC65862-144

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078332
Marketed since
September 5, 2007
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Carvedilol →

Package NDC codes (3)

Package NDCDescriptionSince
65862-144-01100 TABLET, FILM COATED in 1 BOTTLE (65862-144-01)Sep 5, 2007
65862-144-05500 TABLET, FILM COATED in 1 BOTTLE (65862-144-05)Sep 5, 2007
65862-144-991000 TABLET, FILM COATED in 1 BOTTLE (65862-144-99)Sep 5, 2007

Recalls mentioning this NDC

Other Carvedilol products